| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1314342 | Journal of Fluorine Chemistry | 2010 | 5 Pages | 
Abstract
												A highly efficient Suzuki reaction between N-aryltrifluoroacetimidoyl chlorides and aryl boronic acids using Pd(PPh3)4 as a catalyst has been developed. This route allows for selective synthesis of N-aryl trifluoromethylarylketoimines in high yields under mild reaction conditions.
Graphical abstractA highly efficient synthesis of N-aryl trifluoromethylarylketoimines by palladium-catalyzed Suzuki coupling reaction between N-aryltrifluoroacetimidoyl chlorides and aryl boronic acids is described.Figure optionsDownload full-size imageDownload as PowerPoint slide
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											Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Inorganic Chemistry
												
											Authors
												Chun-Lin Li, Mu-Wang Chen, Xing-Guo Zhang, 
											